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ICF syndrome

Introduction: ICF syndrome

Description of ICF syndrome

ICF syndrome (medical condition): A very rare, recessively inherited syndrome...more »

See also:

ICF syndrome:
  »Introduction: ICF syndrome
  »Symptoms of ICF syndrome
  »Treatments for ICF syndrome

ICF syndrome: Variable immunodeficiency with centromeric instability of chromosomes 1, 9, 16 and, less frequently, chromosome 2. Manifestations vary and most common symptoms include facial dysmorphism, mental retardation and prolonged respiratory, cutaneous, and gastrointestinal infections.
Source: Diseases Database

ICF syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for ICF syndrome:

ICF syndrome: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

ICF syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that ICF syndrome, or a subtype of ICF syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list ICF syndrome as a "rare disease".

Source - Orphanet

ICF syndrome as a Disease

ICF syndrome (medical condition): See ICF syndrome (disease information).
  »Introduction: ICF syndrome
  »Symptoms of ICF syndrome
  »Treatments for ICF syndrome

ICF syndrome: Related Diseases

ICF syndrome: ICF syndrome is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: ICF syndrome:

Terms associated with ICF syndrome:

Terms Similar to ICF syndrome:

Source: Diseases Database

Source - NIH

External links related to: ICF syndrome

Source: Diseases Database

Interesting Medical Articles:

Medical dictionaries:

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